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TIMM8A Products

This translocase has similarity to yeast mitochondrial proteins that are involved in the import of metabolite transporters from the cytoplasm into the mitochondrial inner membrane. The gene is mutated in Deafness Dystonia Syndrome (MTS/DFN-1) and it is postulated that MTS/DFN-1 is a mitochondrial disease caused by a defective mitochondrial protein import system.
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43 results for "TIMM8A" in Products

43 results for "TIMM8A" in Products

TIMM8A Products

This translocase has similarity to yeast mitochondrial proteins that are involved in the import of metabolite transporters from the cytoplasm into the mitochondrial inner membrane. The gene is mutated in Deafness Dystonia Syndrome (MTS/DFN-1) and it is postulated that MTS/DFN-1 is a mitochondrial disease caused by a defective mitochondrial protein import system.
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Applications: IHC, WB, ELISA
Reactivity: Human
Applications: WB, ICC/IF
Reactivity: Human
Applications: IHC, ICC/IF
Reactivity: Human
Applications: WB, ELISA, ICC/IF
Reactivity: Human, Mouse, Rat
Applications: WB, ELISA
Reactivity: Human
Applications: WB, ELISA
Reactivity: Human
Applications: IHC
Reactivity: Human
Applications: WB
Applications: PAGE
Applications: IP
Reactivity: Human
Applications: AC
Applications: IHC
Reactivity: Human
Applications: IHC
Reactivity: Human
Applications: IHC
Reactivity: Human
Applications: IHC
Reactivity: Human
Applications: IHC
Reactivity: Human
Applications: IHC
Reactivity: Human
Applications: IHC
Reactivity: Human
Applications: IHC
Reactivity: Human
Applications: IHC
Reactivity: Human
Applications: IHC
Reactivity: Human
Applications: IHC
Reactivity: Human
Applications: IHC
Reactivity: Human
Applications: IHC
Reactivity: Human
Applications: IHC
Reactivity: Human
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